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Published in: BMC Infectious Diseases 1/2019

Open Access 01-12-2019 | Vaccination | Research article

Epidemiological description of a protracted cholera outbreak in Tonj East and Tonj North counties, former Warrap State, South Sudan, May-Oct 2017

Authors: Fred Nsubuga, Stephen Chol Garang, Mathew Tut, David Oguttu, Robert Lubajo, Dennis Lodiongo, Michael Lasuba, Allan Mpairwe

Published in: BMC Infectious Diseases | Issue 1/2019

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Abstract

Background

On 18th May 2017, State Ministry of Health of former Warrap State received a report from Tonj East County of an outbreak of acute watery diarrhoea and vomiting in Makuac payam. We conducted this investigation to confirm the causative organism and describe the epidemiology of the outbreak in order to support evidence-based control measures.

Methods

We defined a suspected case as a resident of Tonj East or Tonj North County with sudden onset of acute watery diarrhoea and vomiting between May 1 and October 15, 2017. A probable case was defined as a suspected case with a positive rapid test for Vibrio cholerae; a confirmed case was a probable case with a positive stool culture for V. cholerae. We conducted systematic case finding by visiting health facilities and villages in the affected payams. We reviewed patient records from 1 May 2017 to 15 October 2017, to identify suspected cholera case-patients. We conducted a descriptive epidemiologic study, examining the distribution of the cases. We computed the attack rates by age, sex, and payam of residence. Case fatality rate was calculated as the ratio of the total number of suspected cholera death to the total number of cholera case-patients. We conducted an oral cholera vaccination campaign after the peak of the outbreak to control and prevent the spread to other payams.

Results

We identified 1451 suspected cholera cases between May and October 2017. Of these, 81% (21/26) had a positive rapid diagnostic test for V. cholerae; out of the 16 rectal swabs transported to the National Public Laboratory, 88% (14/16) were confirmed to be V. cholerae O1 serotype Inaba. The epidemic curve shows continuous common source outbreak with several peaks. The mean age of the case-patients was 24 years (Range: 0.2-75y). The clinical presentations of the case-patients were consistent with cholera. Males had an attack rate of 9.9/10000. The highest attack rate was in ≥30y (14 per 10,000). Among the six payams affected, Makuac had the highest attack rate of 3/100. The case fatality rate (CFR) was 3.0% (44/1451). Paliang and Wunlit had an oral cholera vaccination coverage of ≥100%, while 4 payams had a vaccination coverage of < 90%.

Conclusion

This was a continuous common source cholera outbreak caused by V. cholerae 01 sero type Inaba. We recommended strengthening of the surveillance system to improve early detection and effective response.
Literature
1.
go back to reference Muanprasat C, Chatsudthipong V. Cholera: pathophysiology and emerging therapeutic targets. Future Med Chem. 2013;5(7):781–98.CrossRef Muanprasat C, Chatsudthipong V. Cholera: pathophysiology and emerging therapeutic targets. Future Med Chem. 2013;5(7):781–98.CrossRef
2.
go back to reference Almagro-Moreno S, Pruss K, Taylor RK. Intestinal colonization dynamics of Vibrio cholerae. PLoS Pathog. 2015;11(5):e1004787.CrossRef Almagro-Moreno S, Pruss K, Taylor RK. Intestinal colonization dynamics of Vibrio cholerae. PLoS Pathog. 2015;11(5):e1004787.CrossRef
3.
go back to reference Nandimath VA, Nandimath SA, Swamy CS, Ukrande AR. Epidemiological study of drug resistant cholera in and around Miraj, India. Int J Community Med Public Health. 2017;3(8):2058–63. Nandimath VA, Nandimath SA, Swamy CS, Ukrande AR. Epidemiological study of drug resistant cholera in and around Miraj, India. Int J Community Med Public Health. 2017;3(8):2058–63.
4.
go back to reference Ali M, Lopez AL, You YA, Kim YE, Sah B, Maskery B, et al. The global burden of cholera. Bull World Health Organ. 2012;90:209–18.CrossRef Ali M, Lopez AL, You YA, Kim YE, Sah B, Maskery B, et al. The global burden of cholera. Bull World Health Organ. 2012;90:209–18.CrossRef
5.
go back to reference Gaffga NH, Tauxe RV, Mintz ED. Cholera: a new homeland in Africa? Am J Trop Med. 2007;77(4):705–13.CrossRef Gaffga NH, Tauxe RV, Mintz ED. Cholera: a new homeland in Africa? Am J Trop Med. 2007;77(4):705–13.CrossRef
6.
go back to reference Griffith DC, Kelly-Hope LA, Miller MA. Review of reported cholera outbreaks worldwide, 1995–2005. Am J Trop Med. 2006;75(5):973–7.CrossRef Griffith DC, Kelly-Hope LA, Miller MA. Review of reported cholera outbreaks worldwide, 1995–2005. Am J Trop Med. 2006;75(5):973–7.CrossRef
7.
go back to reference Kur L, Mounir C, Lagu J, Muita M, Rumunu J, Ochieng B, et al. Cholera outbreak-southern Sudan, 2007. Mob Mortal Wkly Rep. 2009;58(13):337–41. Kur L, Mounir C, Lagu J, Muita M, Rumunu J, Ochieng B, et al. Cholera outbreak-southern Sudan, 2007. Mob Mortal Wkly Rep. 2009;58(13):337–41.
8.
go back to reference Ujjiga TTA, Wamala JF, Mogga JJH, Othwonh TO, Mutonga D, Kone-Coulibaly A, et al. Risk factors for sustained cholera transmission, Juba County, South Sudan, 2014. Emerg Infect Dis. 2015;21(10):1849–52.CrossRef Ujjiga TTA, Wamala JF, Mogga JJH, Othwonh TO, Mutonga D, Kone-Coulibaly A, et al. Risk factors for sustained cholera transmission, Juba County, South Sudan, 2014. Emerg Infect Dis. 2015;21(10):1849–52.CrossRef
10.
go back to reference Mukherjee P, Ghosh S, Ramamurthy T, Bhattacharya MK, Nandy RK, Takeda Y, et al. Evaluation of a rapid immunochromatographic dipstick kit for diagnosis of cholera emphasizes its outbreak utility. Jpn J Infect Dis. 2010;63(4):234–8.PubMed Mukherjee P, Ghosh S, Ramamurthy T, Bhattacharya MK, Nandy RK, Takeda Y, et al. Evaluation of a rapid immunochromatographic dipstick kit for diagnosis of cholera emphasizes its outbreak utility. Jpn J Infect Dis. 2010;63(4):234–8.PubMed
11.
go back to reference Debes A, Chakraborty S, Ali M, Sack DA. Manual for detecting Vibrio cholerae O1 and O139 from fecal samples and from environmental water using a dipstick assay; 2014. Debes A, Chakraborty S, Ali M, Sack DA. Manual for detecting Vibrio cholerae O1 and O139 from fecal samples and from environmental water using a dipstick assay; 2014.
12.
go back to reference Ley B, Khatib AM, Thriemer K, von Seidlein L, Deen J, Mukhopadyay A, Chang N-Y, Hashim R, Schmied W, Busch CJL, et al. Evaluation of a rapid dipstick (crystal VC) for the diagnosis of cholera in Zanzibar and a comparison with previous studies. PLoS One. 2012;7(5):e36930.CrossRef Ley B, Khatib AM, Thriemer K, von Seidlein L, Deen J, Mukhopadyay A, Chang N-Y, Hashim R, Schmied W, Busch CJL, et al. Evaluation of a rapid dipstick (crystal VC) for the diagnosis of cholera in Zanzibar and a comparison with previous studies. PLoS One. 2012;7(5):e36930.CrossRef
13.
go back to reference Swerdlow DL, Greene KD, Tauxe RV, Wells JG, Bean NH, Ries AA, et al. Waterborne transmission of epidemic cholera in Trujillo, Peru: lessons for a continent at risk. Lancet. 1992;340(8810):28–32.CrossRef Swerdlow DL, Greene KD, Tauxe RV, Wells JG, Bean NH, Ries AA, et al. Waterborne transmission of epidemic cholera in Trujillo, Peru: lessons for a continent at risk. Lancet. 1992;340(8810):28–32.CrossRef
14.
go back to reference Hendrix TR. The pathophysiology of cholera. J Urban Health. 1971;47(10):1169–80. Hendrix TR. The pathophysiology of cholera. J Urban Health. 1971;47(10):1169–80.
15.
go back to reference Reidl J, Klose KE. Vibrio cholerae and cholera: out of the water and into the host. FEMS Microbiol Rev. 2002;26(2):125–39.CrossRef Reidl J, Klose KE. Vibrio cholerae and cholera: out of the water and into the host. FEMS Microbiol Rev. 2002;26(2):125–39.CrossRef
16.
go back to reference Abubakar A, Azman AS, Rumunu J, Ciglenecki I, Helderman T, West H, Lessler J, et al. The first use of the global oral cholera vaccine emergency stockpile: lessons from South Sudan. PLoS Med. 2015;12(11):e1001901.CrossRef Abubakar A, Azman AS, Rumunu J, Ciglenecki I, Helderman T, West H, Lessler J, et al. The first use of the global oral cholera vaccine emergency stockpile: lessons from South Sudan. PLoS Med. 2015;12(11):e1001901.CrossRef
17.
go back to reference Taneja N, Biswal M, Tarai B, Sharma M. Emergence of Vibrio cholerae O1 biotype E1 Tor serotype Inaba in North India. Jpn J Infect Dis. 2005;58(4):238.PubMed Taneja N, Biswal M, Tarai B, Sharma M. Emergence of Vibrio cholerae O1 biotype E1 Tor serotype Inaba in North India. Jpn J Infect Dis. 2005;58(4):238.PubMed
18.
go back to reference Mahapatra T, Mahapatra S, Babu GR, Tang W, Banerjee B, Mahapatra U, et al. Cholera outbreaks in south and Southeast Asia: descriptive analysis, 2003–2012. Jpn J Infect Dis. 2014;67(3):145–56.CrossRef Mahapatra T, Mahapatra S, Babu GR, Tang W, Banerjee B, Mahapatra U, et al. Cholera outbreaks in south and Southeast Asia: descriptive analysis, 2003–2012. Jpn J Infect Dis. 2014;67(3):145–56.CrossRef
19.
go back to reference Snow J. On the mode of communication of cholera: John: Churchill; 1855. Snow J. On the mode of communication of cholera: John: Churchill; 1855.
20.
go back to reference Iijima Y, Oundo J, Taga K, Saidi S, Honda T. Simultaneous outbreak due to Vibrio cholerae and Shigella dysenteriae in Kenya. Lancet. 1995;345(8941):69–70.CrossRef Iijima Y, Oundo J, Taga K, Saidi S, Honda T. Simultaneous outbreak due to Vibrio cholerae and Shigella dysenteriae in Kenya. Lancet. 1995;345(8941):69–70.CrossRef
22.
go back to reference Oladele DA, Oyedeji KS, Niemogha M-T, Nwaokorie F, Bamidele M, Musa AZ, et al. An assessment of the emergency response among health workers involved in the 2010 cholera outbreak in northern Nigeria. J Infect Public Health. 2012;5(5):346–53.CrossRef Oladele DA, Oyedeji KS, Niemogha M-T, Nwaokorie F, Bamidele M, Musa AZ, et al. An assessment of the emergency response among health workers involved in the 2010 cholera outbreak in northern Nigeria. J Infect Public Health. 2012;5(5):346–53.CrossRef
23.
go back to reference Mahamud AS, Ahmed JA, Nyoka R, Auko E, Kahi V, Ndirangu J, et al. Epidemic cholera in Kakuma refugee camp, Kenya, 2009: the importance of sanitation and soap. J Infect Dev Ctries. 2011;6(03):234–41. Mahamud AS, Ahmed JA, Nyoka R, Auko E, Kahi V, Ndirangu J, et al. Epidemic cholera in Kakuma refugee camp, Kenya, 2009: the importance of sanitation and soap. J Infect Dev Ctries. 2011;6(03):234–41.
25.
go back to reference Date KA, Vicari A, Hyde TB, Mintz E, Danovaro-Holliday MC, Henry A, et al. Considerations for oral cholera vaccine use during outbreak after earthquake in Haiti, 2010− 2011. Emerg Infect Dis. 2011;17(11):2105.CrossRef Date KA, Vicari A, Hyde TB, Mintz E, Danovaro-Holliday MC, Henry A, et al. Considerations for oral cholera vaccine use during outbreak after earthquake in Haiti, 2010− 2011. Emerg Infect Dis. 2011;17(11):2105.CrossRef
Metadata
Title
Epidemiological description of a protracted cholera outbreak in Tonj East and Tonj North counties, former Warrap State, South Sudan, May-Oct 2017
Authors
Fred Nsubuga
Stephen Chol Garang
Mathew Tut
David Oguttu
Robert Lubajo
Dennis Lodiongo
Michael Lasuba
Allan Mpairwe
Publication date
01-12-2019
Publisher
BioMed Central
Published in
BMC Infectious Diseases / Issue 1/2019
Electronic ISSN: 1471-2334
DOI
https://doi.org/10.1186/s12879-018-3640-5

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